US2012100617A1PendingUtilityA1

Pichia pastoris loci encoding enzymes in the adenine biosynthetic pathway

Assignee: NETT JUERGENPriority: Oct 25, 2010Filed: Oct 13, 2011Published: Apr 26, 2012
Est. expiryOct 25, 2030(~4.3 yrs left)· nominal 20-yr term from priority
C12N 15/815C12N 9/1014C12N 9/1077C12N 9/88C12N 9/93C12N 15/52C12Y 201/02002C12Y 204/02014C12Y 403/02002C12Y 603/02017C12Y 603/03001C12Y 603/04004C12Y 603/04013C12Y 603/05003
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Claims

Abstract

Disclosed are the ADE3, ADE4, ADE5, 7, ADE6, ADE8, ADE12, and ADE13 genes encoding various enzymes in the adenine biosynthesis pathway of Pichia pastoris . The loci in the Pichia pastoris genome encoding these enzymes are useful sites for stable integration of heterologous nucleic acid molecules into the Pichia pastoris genome. The genes or gene fragments encoding the particular enzymes, which may be used as selection markers for constructing recombinant Pichia pastoris.

Claims

exact text as granted — not AI-modified
1 . A plasmid vector that is capable of integrating into a  Pichia pastoris  locus selected from the group consisting of ADE3, ADE4, ADE5, 7, ADE6, ADE8, ADE12, and ADE13. 
     
     
         2 . The plasmid vector of  claim 1  comprising a nucleotide sequence with at least 95% to a nucleotide sequence comprising at least 25, 50, 75, 100, 125, 150, 175, or 200 contiguous nucleotides of SEQ ID NO:1, 2, 3, 4, 5, 6, and 7. 
     
     
         3 . The plasmid vector of  claim 1 , wherein the plasmid vector further includes a nucleic acid molecule encoding a heterologous peptide, protein, or functional nucleic acid molecule of interest. 
     
     
         4 . A method for producing a recombinant  Pichia pastoris  auxotrophic for adenine, comprising:
 transforming a  Pichia pastoris  host cell with the plasmid vector capable of integrating into the ADE3, ADE4, ADE5, 7, ADE6, ADE8, ADE12, or ADE13 locus, wherein the plasmid vector integrates into the locus to disrupt or delete the locus to produce the recombinant  Pichia pastoris  auxotrophic for adenine.   
     
     
         5 . A recombinant  Pichia pastoris  produced by the method of  claim 4 . 
     
     
         6 . A nucleic acid molecule comprising a nucleotide sequence with at least 95% identity to a nucleotide sequence comprising at least 25, 50, 75, 100, 125, 150, 175, or 200 contiguous nucleotides of SEQ ID NO:1, 2, 3, 4, 5, 6, and 7. 
     
     
         7 . A plasmid vector comprising a nucleic acid sequence encoding a  Pichia pastoris  enzyme selected from the group consisting of Ade3p, Ade4p, Ade5,7p, Ade6p, Ade8p, Ade12p, and Ade13p. 
     
     
         8 . The plasmid vector of  claim 5  comprising a nucleotide sequence with at least 95% identity to a nucleotide sequence comprising at least 25, 50, 75, 100, 125, 150, 175, or 200 contiguous nucleotides of SEQ ID NO:1, 2, 3, 4, 5, 6, and 7. 
     
     
         9 . A method for rendering a recombinant  Pichia pastoris  that is auxotrophic for adenine into a recombinant  Pichia pastoris  prototrophic for adenine comprising:
 (a) providing a recombinant ade2, ade4, ade5, 7, ade6, ade8, ade12, or ade13  Pichia pastoris  host cell auxotrophic for adenine; and   (b) transforming the recombinant  Pichia pastoris  with a plasmid vector encoding the enzyme that complements the auxotrophy to render the recombinant  Pichia pastoris  auxotrophic for adenine into a  Pichia pastoris  prototrophic for adenine.   
     
     
         10 . The method of  claim 9 , wherein the host cell auxotrophic for adenine has a deletion or disruption of the ADE2, ADE4, ADE5, 7, ADE6, ADE8, ADE12, or ADE13 locus. 
     
     
         11 . The method of  claim 9 , wherein the plasmid vector encoding the enzyme that complements the auxotrophy integrates into a location in the genome of the host cell. 
     
     
         12 . The method of  claim 9 , wherein the location is not the ADE2, ADE4, ADE5, 7, ADE6, ADE8, ADE12, or ADE13 locus.

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